Modulating the Structure and Composition of Single-Atom Electrocatalysts for CO2 reduction.

Electrochemical CO2 reduction reaction (eCO2 RR) is a promising strategy to achieve carbon cycling by converting CO2 into value-added products under mild reaction conditions. Recently, single-atom catalysts (SACs) have shown enormous potential in eCO2 RR due to their high utilization of metal atoms and flexible coordination structures. In this work, the recent progress in SACs for eCO2 RR is outlined, with detailed discussions on the interaction between active sites and CO2 , especially the adsorption/activation behavior of CO2 and the effects of the electronic structure of SACs on eCO2 RR. Three perspectives form the starting point: 1) Important factors of SACs for eCO2 RR; 2) Typical SACs for eCO2 RR; 3) eCO2 RR toward valuable products. First, how different modification strategies can change the electronic structure of SACs to improve catalytic performance is discussed; Second, SACs with diverse supports and how supports assist active sites to undergo catalytic reaction are introduced; Finally, according to various valuable products from eCO2 RR, the reaction mechanism and measures which can be taken to improve the selectivity of eCO2 RR are discussed. Hopefully, this work can provide a comprehensive understanding of SACs for eCO2 RR and spark innovative design and modification ideas to develop highly efficient SACs for CO2 conversion to various valuable fuels/chemicals.

High Formate Selectivity and Deactivation Mechanism of CuS Nanoparticles in CO2 Electrocatalytic Reduction Reaction.

CO2 electroreduction into liquid fuels is of broad interest and benefits reducing the energy crisis and environment burdens. CuS has been reported to be a desirable candidate for CO2 electroreduction into formate; however, its formate selectivity and stability are still far from the demands of practical application. Herein, we report CuS nanoparticles exhibiting good Faradaic efficiency of formate (about 98 %) in CO2 electroreduction and its deactivation mechanism during the reaction. The deactivation of CuS was found to be associated with the reconstruction and S loss of CuS, which deteriorates the Faradaic efficiency of formate. Combined with ionic and gas analyses, the S atom in CuS was lost in the form of H2 S, SO2 , and SO4 2- , followed by the reconstruction of CuS into copper oxides. Such a catalyst reconstruction facilitates electroreductions of CO2 and H2 O, respectively, into CO and H2 , etc., resulting in the degradation of catalytical performance of CO2 electroreduction into formate. This work reveals the important role of S loss and reconstruction of metal sulfide catalysts during the electroreduction reaction, which may benefit the further development of CuS-based electro-catalyst for CO2 electroreduction.

Enhanced toluene oxidation by photothermal synergetic catalysis on manganese oxide embedded with Pt single-atoms.

The degradation of volatile organic compounds (VOCs) at low temperature remains a big challenge. Photothermal catalysis coupling the advantages of photocatalysis and thermocatalysis is promising to address this issue. However, there is still a long way to construct highly active catalysts and deeply understand the mechanism of photothermal catalysis. Herein, maganese oxide (MnO2)catalysts embedded with Pt single-atoms (0.11 wt% Pt) have achieved greatly enhanced toluene conversion of 95%, far surpassing most supported Pt photothermal catalysts. The excellent catalytic activity has been disclosed to derive from the synergetic effect oflight-driven thermocatalysis and photocatalysis. The light-driven thermocatalysis predominates and the strong electron transfer from Pt single-atoms to MnO2 improves the activity of surface lattice oxygen to boost the generation of benzoic acid and the mineralization of toluene. Meanwhile, in photocatalytic process, Pt single-atoms accelerate the generation of superoxide radicals (O2-), which facilitate the ring-opening and deep oxidation of toluene. This understanding on the photothermal synergetic mechanism will inspire the design of highly efficient catalysts for VOCs oxidation.

Mild generation of surface oxygen vacancies on CeO2 for improved CO2 photoreduction activity.

The vacancy defects of semiconductor photocatalysts play key roles in enhancing their photocatalytic CO2 reduction activity. In this work, CeO2 was chosen as a model catalyst and oxygen vacancies were introduced on its surface by a facile and mild oxalic acid treatment followed by moderate heating in N2. Such a treatment resulted in a much increased ratio of Ce3+/Ce4+ in CeO2, and the oxygen vacancy-enriched CeO2 showed remarkably enhanced photocatalytic activity in CO2 reduction, with CO being the dominant reduction product, whose yield was about 8 times that on the pristine CeO2. In situ FT-IR spectra showed that the abundant oxygen vacancies substantially improved the CO2 adsorption/activation on the surface of CeO2, which facilitated the subsequent reduction of CO2. However, the carbonates strongly adsorbed on the photocatalyst surface might be the main obstacle to maintaining the high CO2 reduction activity and stability of CeO2 with O vacancies.

Electron Configuration Modulation of Nickel Single Atoms for Elevated Photocatalytic Hydrogen Evolution.

The emerging metal single-atom catalyst has aroused extensive attention in multiple fields, such as clean energy, environmental protection, and biomedicine. Unfortunately, though it has been shown to be highly active, the origins of the activity of the single-atom sites remain unrevealed to date owing to the lack of deep insight on electronic level. Now, partially oxidized Ni single-atom sites were constructed in polymeric carbon nitride (CN), which elevates the photocatalytic performance by over 30-fold. The 3d orbital of the partially oxidized Ni single-atom sites is filled with unpaired d-electrons, which are ready to be excited under irradiation. Such an electron configuration results in elevated light response, conductivity, charge separation, and mobility of the photocatalyst concurrently, thus largely augmenting the photocatalytic performance.